Blood group O has been associated with an increased bleeding tendency due to lower von
Willebrand factor (VWF) and factor VIII (FVIII) levels. We explored whether blood group O is …

A State of the Art lecture titled “Investigating Patients for Bleeding Disorders When Most of
the Usual Ones Have Been Ruled Out” was presented at the International Society on …

Background Hemorrhage is a significant cause of death in trauma patients. There is
evidence that individuals with blood group O have higher rates of non-traumatic …

Cell shape is critical for the proper function of every cell in every tissue in the body. This is
especially true for the highly morphologically diverse neural and glia cells of the central …

VWF is a procoagulant protein that plays a central role in the initiation of platelets aggregate
formation and thrombosis. While von Willebrand disease has long been known to result from …

Hemophilia A is an inherited X-linked recessive bleeding disorder caused by deficient
activity of blood coagulation factor VIII (FVIII). In addition, hemophilia patients show …

Most people with von Willebrand disease (VWD) have a partial quantitative deficiency of
plasma von Willebrand factor (VWF) or type 1 VWD. In contrast to type 2 and type 3 VWD …

Introduction Primary blood coagulation and wound sealing are orchestrated by von
Willebrand factor (VWF), a large multimeric glycoprotein. Upon release of arginine …

Background The clinical phenotype of hemophilia A (HA) does not always correlate with
severity. Similarly, the presence of inhibitors does not necessarily increase the risk of …

Актуальность исследования. Актуальной проблемой современной медицины является
исследование эндокардитов как причины развития тромбоэмболических осложнений …